Constructing a slippery lubricant-infused surface (SLIS) whose internal microstructure and surface properties can be fully repaired helps to improve its property stability and extend technological implications but has presented a huge challenge. A class of fully repairable slippery organogel surfaces (SOSs), which uses microstructured paraffin as reconfigurable supporting structure and silicone oil as lubricant dispersion medium, is reported here. Attributed to nearly 90 wt % of silicone oil stored in the slippery organogel system and good compatibility with the paraffin-based framework, SOSs combine continuous lubricity and reliable lubricant storage stability. Furthermore, the thermally sensitive paraffin-based framework can quickly switch between solid supporting structure and liquid solution according to the ambient temperature, thereby achieving rapid regeneration of microstructure. This unique system consisting of reconfigurable framework and flowable lubricant derives two types of repairs aimed at varying degrees of damage. Significantly, the easy-to-prepare SOS, on the other hand, allows the adoption of various substrate surfaces for different purposes to form an antiadhesion coating and exhibits excellent antistain, antialgae, and anti-icing performance, thus greatly improving the flexibility of such materials in practical applications.Nickel oxide (NiO) is considered one of the most promising positive anode materials for electrochromic supercapacitors. Nevertheless, a detailed mechanism of the electrochromic and energy storage process has yet to be unraveled. In this research, the charge storage mechanism of a NiO electrochromic electrode was investigated by combining the in-depth experimental and theoretical analyses. Experimentally, a kinetic analysis of the Li-ion behavior based on the cyclic voltammetry curves reveals the major contribution of surface capacitance versus total capacity, providing fast reaction kinetics and a highly reversible electrochromic performance. Theoretically, our model uncovers that Li ions prefer to adsorb at fcc sites on the NiO(1 1 1) surface, then diffuse horizontally over the plane, and finally migrate in the bulk. More significantly, the calculated theoretical surface capacity (106 mA h g-1) accounts for about 77.4% of the total experimental capacity (137 mA h g-1), indicating that the surface storage process dominates the whole charge storage, which is in accordance with the experimental results. This work provides a fundamental understanding of transition-metal oxides for application in electrochromic supercapacitors and can also promote the exploration of novel electrode materials for high-performance electrochromic supercapacitors.Interfacing two-dimensional graphene oxide (GO) platelets with one-dimensional zinc oxide nanorods (ZnO) would create mixed-dimensional heterostructures suitable for modern optoelectronic devices. However, there remains a lack in understanding of interfacial chemistry and wettability in GO-coated ZnO nanorods heterostructures. Here, we propose a hydroxyl-based dissociation-exchange mechanism to understand interfacial interactions responsible for GO adsorption onto ZnO nanorods hydrophobic substrates. The proposed mechanism initiated from mixing GO suspensions with various organics would allow us to overcome the poor wettability (θ ? 140.5°) of the superhydrophobic ZnO nanorods to the drop-casted GO. The addition of different classes of organics into the relatively high pH GO suspension with a volumetric ratio of 13 (organic-to-GO) is believed to introduce free radicals (-OH and -COOH), which consequently result in enhancing adhesion (chemisorption) between ZnO nanorods and GO platelets. The wettability study shows as high as 75% reduction in the contact angle (θ = 35.5°) when the GO suspension is mixed with alcohols (e.g., ethanol) prior to interfacing with ZnO nanorods. The interfacial chemistry developed here brings forth a scalable tool for designing graphene-coated ZnO heterojunctions for photovoltaics, photocatalysis, biosensors, and UV detectors.Membranes showing monomodal pore size distributions with mean pore diameters of 23, 33, and 60 nm are chemically functionalized using silanes with varying chain length and functional groups like amino, alkyl, phenyl, sulfonate, and succinic anhydrides. Their influence on the morphology, pore structure, and gas flow is investigated. For this, single-gas permeation measurements at pressures around 0.1 MPa are performed at temperatures ranging from 273 to 353 K using He, Ne, Ar, N2, CO, CO2, CH4, C2H4, C2H6, and C3H8. Results show pore size and pore volume linearly depending on the length of functional molecules, as expected for monolayer deposition. However, the gas flow through functionalized membranes is disproportionally decreased up to a factor of around 10. Hence, the decreased pore size and pore volume cannot explain the large decrease in flow. https://www.selleckchem.com/products/hs-173.html Furthermore, there is no specific dependency between the decrease in flow and temperature or gas type other than the relation proposed by Knudsen (√RTM)-1. Considering the large variety of functional molecules used, it is very surprising that no correlations between the type of functional group and the flow have been found. The decrease in flow, however, is strongly dependent on the chain length of the silanes (factor of 10 at ?2 nm length). This leads to the conclusion that the observed effect is not caused by sorption driven processes. It is proposed that steric interactions between functional groups and gas molecules lead to increased residence times on the surface and longer molecular trajectories, which, in turn, lead to a decrease in flow. In membrane design, any surface modification should, therefore, make use of functionalizing agents with chain length as short as possible.Although the pronounced piezoelectricity was obtained in (K, Na)NbO3 piezoceramics with the phase boundary engineering (PBE), the physical mechanisms remain pending. Here, we revealed for the first time how PBE influences the piezoelectric properties through synergetic contributions. Cryogenic experiments confirm that PBE constructs a phase coexistence, consisting of rhombohedral (R), orthorhombic (O), and tetragonal (T) phases, with a structural softening, by which a high piezoelectric coefficient d33 of 555 pC/N and the enhanced temperature stability of strain are achieved. The phenomenological theory and transmission electron microscopy demonstrate that the superior d33 hinges on the flattened Gibbs free energy and the abundant nanodomains (10-80 nm), which induce the enhanced permittivity and the coexisting single domain and multidomain zones, respectively. In particular, we disclosed a trade-off relationship between ferroelectric domains and polar nanoregions (PNRs) and found the "double-edged sword" role of PNRs in the piezoelectricity enhancement.